List of variants in gene TYR reported as uncertain significance by Eurofins Ntd Llc (ga)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000372.5(TYR):c.1205G>A (p.Arg402Gln)	rs1126809	0.17677
NM_000372.5(TYR):c.665T>C (p.Ile222Thr)	rs34878847	0.00096
NM_000372.5(TYR):c.504C>T (p.Asn168=)	rs148813091	0.00051
NM_000372.5(TYR):c.1067A>T (p.Asp356Val)	rs180801021	0.00037
NM_000372.5(TYR):c.1446G>C (p.Ala482=)	rs3913543	0.00022
NM_000372.5(TYR):c.1161T>C (p.Leu387=)	rs141967840	0.00011
NM_000372.5(TYR):c.759A>T (p.Gly253=)	rs200936835	0.00003
NM_000372.5(TYR):c.1037-10dup	rs747032303
NM_000372.5(TYR):c.1136G>C (p.Gly379Ala)	rs886044493
NM_000372.5(TYR):c.1234C>G (p.Pro412Ala)	rs797046081
NM_000372.5(TYR):c.1413G>A (p.Ala471=)	rs3913544
NM_000372.5(TYR):c.505_507del (p.Asp169del)	rs794726885

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